HuGE Literature Finder
Records 1-30
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Panel gene profiling of small bowel adenocarcinoma, results from the NADEGE prospective cohort.
International journal of cancer 2020 Nov . Aparicio Thomas, Svrcek Magali, Henriques Julie, Afchain Pauline, Lièvre Astrid, Tougeron David, Gagniere Johan, Terrebonne Eric, Piessen Guillaume, Legoux Jean-Louis, Lecaille Cédric, Pocard Marc, Gornet Jean-Marc, Zaanan Aziz, Lavau-Denes Sandrine, Lecomte Thierry, Deutsch David, Vernerey Dewi, Laurent Puig Pier |
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The prognostic role of BRAF and WNT pathways activation in kinase inhibitors-naïve clinical stage III cutaneous melanoma.
Melanoma research 2020 Feb . Kowalik Artur, Jurkowska Monika, Mierzejewska Ewa, Lugowska Iwona, Gos Aleksandra, Szumera-Cieckiewicz Anna, Zieba Sebastian, Kosela-Paterczyk Hanna, van der Oord Joost, Debiec-Rychter Maria, Szamotulska Katarzyna, Siedlecki Janusz, Rutkowski Pio |
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Inactivating mutations in genes encoding for components of the BAF/PBAF complex and immune-checkpoint inhibitor outcome.
Biomarker research 2020 8 26. Courtet Kevin, Laizet Yec'han, Lucchesi Carlo, Bessede Alban, Italiano Antoi |
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Genetic abnormalities in a large cohort of Coffin-Siris syndrome patients.
Journal of human genetics 2019 Sep . Sekiguchi Futoshi, Tsurusaki Yoshinori, Okamoto Nobuhiko, Teik Keng Wee, Mizuno Seiji, Suzumura Hiroshi, Isidor Bertrand, Ong Winnie Peitee, Haniffa Muzhirah, White Susan M, Matsuo Mari, Saito Kayoko, Phadke Shubha, Kosho Tomoki, Yap Patrick, Goyal Manisha, Clarke Lorne A, Sachdev Rani, McGillivray George, Leventer Richard J, Patel Chirag, Yamagata Takanori, Osaka Hitoshi, Hisaeda Yoshiya, Ohashi Hirofumi, Shimizu Kenji, Nagasaki Keisuke, Hamada Junpei, Dateki Sumito, Sato Takashi, Chinen Yasutsugu, Awaya Tomonari, Kato Takeo, Iwanaga Kougoro, Kawai Masahiko, Matsuoka Takashi, Shimoji Yoshikazu, Tan Tiong Yang, Kapoor Seema, Gregersen Nerine, Rossi Massimiliano, Marie-Laure Mathieu, McGregor Lesley, Oishi Kimihiko, Mehta Lakshmi, Gillies Greta, Lockhart Paul J, Pope Kate, Shukla Anju, Girisha Katta Mohan, Abdel-Salam Ghada M H, Mowat David, Coman David, Kim Ok Hwa, Cordier Marie-Pierre, Gibson Kate, Milunsky Jeff, Liebelt Jan, Cox Helen, El Chehadeh Salima, Toutain Annick, Saida Ken, Aoi Hiromi, Minase Gaku, Tsuchida Naomi, Iwama Kazuhiro, Uchiyama Yuri, Suzuki Toshifumi, Hamanaka Kohei, Azuma Yoshiteru, Fujita Atsushi, Imagawa Eri, Koshimizu Eriko, Takata Atsushi, Mitsuhashi Satomi, Miyatake Satoko, Mizuguchi Takeshi, Miyake Noriko, Matsumoto Naomic |
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Intraventricular meningiomas frequently harbor NF2 mutations but lack common genetic alterations in TRAF7, AKT1, SMO, KLF4, PIK3CA, and TERT.
Acta neuropathologica communications 2019 Aug 7 (1): 140. Jungwirth Gerhard, Warta Rolf, Beynon Christopher, Sahm Felix, von Deimling Andreas, Unterberg Andreas, Herold-Mende Christel, Jungk Christi |
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Targeted next generation sequencing identified a high frequency genetic mutated profile in wood smoke exposure-related lung adenocarcinoma patients.
Oncotarget 2018 Jul 9 (55): 30499-30512. Soca-Chafre Giovanny, Hernández-Pedro Norma, Aviles-Salas Alejandro, Versón Carmen Alaez, Sánchez Karol Carrillo, Cardona Andrés F, Avila-Moreno Federico, Barrios-Bernal Pedro, Flores-Estrada Diana, Arrieta Osc |
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Mutations in BRCA1, BRCA2, and PALB2, and a panel of 50 cancer-associated genes in pancreatic ductal adenocarcinoma.
Scientific reports 2018 May 8 (1): 8105. Takeuchi Shoko, Doi Manami, Ikari Naoki, Yamamoto Masakazu, Furukawa To |
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Clinical and molecular characterization of neurofibromatosis in southern Brazil.
Expert review of molecular diagnostics 2018 Apr 1-10. Rosset Clévia, Vairo Filippo, Cristina Bandeira Isabel, Fonini Maievi, Netto Cristina Brinckmann Oliveira, Ashton-Prolla Patric |
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TERT promoter wild-type glioblastomas show distinct clinical features and frequent PI3K pathway mutations.
Acta neuropathologica communications 2018 10 6 (1): 106. Williams Erik A, Miller Julie J, Tummala Shilpa S, Penson Tristan, Iafrate A John, Juratli Tareq A, Cahill Daniel |
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Value of a molecular screening program to support clinical trial enrollment in Asian cancer patients: The Integrated Molecular Analysis of Cancer (IMAC) Study.
International journal of cancer 2018 05 142 (9): 1890-1900. Heong Valerie, Syn Nicholas L, Lee Xiao Wen, Sapari Nur Sabrina, Koh Xue Qing, Adam Isa Zul Fazreen, Sy Lim Joey, Lim Diana, Pang Brendan, Thian Yee Liang, Ng Lai Kuan, Wong Andrea L, Soo Ross Andrew, Yong Wei Peng, Chee Cheng Ean, Lee Soo-Chin, Goh Boon-Cher, Soong Richie, Tan David S |
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Variation in SWI/SNF Chromatin Remodeling Complex Proteins is Associated with Alcohol Dependence and Antisocial Behavior in Human Populations.
Alcoholism, clinical and experimental research 2017 Dec 41 (12): 2033-2040. Mathies Laura D, Aliev Fazil, , Davies Andrew G, Dick Danielle M, Bettinger Jill |
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Epithelial-Myoepithelial Carcinoma: Frequent Morphologic and Molecular Evidence of Preexisting Pleomorphic Adenoma, Common HRAS Mutations in PLAG1-intact and HMGA2-intact Cases, and Occasional TP53, FBXW7, and SMARCB1 Alterations in High-grade Cases.
The American journal of surgical pathology 2017 Nov . El Hallani Soufiane, Udager Aaron M, Bell Diana, Fonseca Isabel, Thompson Lester D R, Assaad Adel, Agaimy Abbas, Luvison Alyssa M, Miller Caitlyn, Seethala Raja R, Chiosea Simi |
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Frequent IDH2 R172 Mutations in Undifferentiated and Poorly-Differentiated Sinonasal Carcinomas.
The Journal of pathology 2017 May . Dogan Snjezana, Chute Deborah J, Xu Bin, Ptashkin Ryan N, Chandramohan Raghu, Casanova-Murphy Jacklyn, Nafa Khedoudja, Bishop Justin A, Chiosea Simion I, Stelow Edward B, Ganly Ian, Pfister David G, Katabi Nora, Ghossein Ronald A, Berger Michael |
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Increased genomic burden of germline copy number variants is associated with early onset breast cancer: Australian breast cancer family registry.
Breast cancer research : BCR 2017 Mar 19 (1): 30. Walker Logan C, Pearson John F, Wiggins George A R, Giles Graham G, Hopper John L, Southey Melissa |
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Molecular alterations of coexisting thyroid papillary carcinoma and anaplastic carcinoma: identification of TERT mutation as an independent risk factor for transformation.
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2017 11 30 (11): 1527-1537. Oishi Naoki, Kondo Tetsuo, Ebina Aya, Sato Yukiko, Akaishi Junko, Hino Rumi, Yamamoto Noriko, Mochizuki Kunio, Nakazawa Tadao, Yokomichi Hiroshi, Ito Koichi, Ishikawa Yuichi, Katoh Ryoh |
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Targeted molecular profiling of rare genetic alterations in colorectal cancer using next-generation sequencing.
Medical oncology (Northwood, London, England) 2016 Oct 33 (10): 106. Jauhri Mayank, Bhatnagar Akanksha, Gupta Satish, Shokeen Yogender, Minhas Sachin, Aggarwal Shy |
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SMARCB1/INI1 Involvement in Pediatric Chordoma: A Mutational and Immunohistochemical Analysis.
The American journal of surgical pathology 2016 Sep . Antonelli Manila, Raso Alessandro, Mascelli Samantha, Gessi Marco, Nozza Paolo, Coli Antonella, Gardiman Marina P, Arcella Antonietta, Massimino Maura, Buttarelli Francesca R, Giangaspero Feli |
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Cribriform neuroepithelial tumor (crinet): Molecular characterization of a smarcb1-deficient non-rhabdoid tumor with favorable long-term outcome.
Brain pathology (Zurich, Switzerland) 2016 Jul . Johann Pascal D, Hovestadt Volker, Thomas Christian, Jeibmann Astrid, Heß Katharina, Bens Susanne, Oyen Florian, Hawkins Cynthia, Pierson Christopher R, Aldape Kenneth, Pyo Kim Sang, Widing Eva, Sumerauer David, Hauser Péter, van Landeghem Frank, Ryzhova Marina, Korshunov Andrey, Capper David, Jones David T W, Pfister Stefan M, Schneppenheim Reinhard, Siebert Reiner, Paulus Werner, Frühwald Michael C, Kool Marcel, Hasselblatt Mart |
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Multifocal Nerve Lesions and LZTR1 Germline Mutations in Segmental Schwannomatosis.
Annals of neurology 2016 Jul . Farschtschi Said, Mautner Victor-Felix, Pham Mirko, Nguyen Rosa, Kehrer-Sawatzki Hildegard, Hutter Sonja, Friedrich Reinhard E, Schulz Alexander, Morrison Helen, Jones David T W, Bendszus Martin, Bäumer Phili |
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Outcome of extracranial malignant rhabdoid tumours in children registered in the European Paediatric Soft Tissue Sarcoma Study Group Non-Rhabdomyosarcoma Soft Tissue Sarcoma 2005 Study-EpSSG NRSTS 2005.
European journal of cancer (Oxford, England : 1990) 2016 Apr 60 69-82. Brennan Bernadette, De Salvo Gian Luca, Orbach Daniel, De Paoli Angela, Kelsey Anna, Mudry Peter, Francotte Nadine, Van Noesel Max, Bisogno Gianni, Casanova Michela, Ferrari Andr |
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Atypical Teratoid/Rhabdoid Tumors Are Comprised of Three Epigenetic Subgroups with Distinct Enhancer Landscapes.
Cancer cell 2016 Feb . Johann Pascal D, Erkek Serap, Zapatka Marc, Kerl Kornelius, Buchhalter Ivo, Hovestadt Volker, Jones David T W, Sturm Dominik, Hermann Carl, Segura Wang Maia, Korshunov Andrey, Rhyzova Marina, Gröbner Susanne, Brabetz Sebastian, Chavez Lukas, Bens Susanne, Gröschel Stefan, Kratochwil Fabian, Wittmann Andrea, Sieber Laura, Geörg Christina, Wolf Stefan, Beck Katja, Oyen Florian, Capper David, van Sluis Peter, Volckmann Richard, Koster Jan, Versteeg Rogier, von Deimling Andreas, Milde Till, Witt Olaf, Kulozik Andreas E, Ebinger Martin, Shalaby Tarek, Grotzer Michael, Sumerauer David, Zamecnik Josef, Mora Jaume, Jabado Nada, Taylor Michael D, Huang Annie, Aronica Eleonora, Bertoni Anna, Radlwimmer Bernhard, Pietsch Torsten, Schüller Ulrich, Schneppenheim Reinhard, Northcott Paul A, Korbel Jan O, Siebert Reiner, Frühwald Michael C, Lichter Peter, Eils Roland, Gajjar Amar, Hasselblatt Martin, Pfister Stefan M, Kool Marc |
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Identification of the BRAF V600E mutation in gastroenteropancreatic neuroendocrine tumors.
Oncotarget 2015 Dec . Park Charny, Ha Sang Yun, Kim Seung Tae, Kim Hee Cheol, Heo Jin Seok, Park Young Suk, Lauwers Gregory, Lee Jeeyun, Kim Kyoung-M |
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Genetic variants in the SWI/SNF complex and smoking collaborate to modify the risk of pancreatic cancer in a Chinese population.
Molecular carcinogenesis 2015 Sep 54 (9): 761-8. Zhu Beibei, Tian Jing, Zhong Rong, Tian Yao, Chen Wei, Qian Jiaming, Zou Li, Xiao Min, Shen Na, Yang Hong, Lou Jiao, Qiu Qian, Ke Juntao, Lu Xinghua, Song Wei, Li Hui, Liu Li, Wang Li, Miao Xiaopi |
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Mutations in LZTR1 add to the complex heterogeneity of schwannomatosis.
Neurology 2015 Jan 84 (2): 141-7. Smith Miriam J, Isidor Bertand, Beetz Christian, Williams Simon G, Bhaskar Sanjeev S, Richer Wilfrid, O'Sullivan James, Anderson Beverly, Daly Sarah B, Urquhart Jill E, Fryer Alan, Rustad Cecilie F, Mills Samantha J, Samii Amir, du Plessis Daniel, Halliday Dorothy, Barbarot Sebastien, Bourdeaut Franck, Newman William G, Evans D Gare |
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Mutational profiling of familial male breast cancers reveals similarities with luminal A female breast cancer with rare TP53 mutations.
British journal of cancer 2014 Dec 111 (12): 2351-60. Deb S, Wong S Q, Li J, Do H, Weiss J, Byrne D, Chakrabarti A, Bosma T, , Fellowes A, Dobrovic A, Fox S |
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Genotype-phenotype correlation of Coffin-Siris syndrome caused by mutations in SMARCB1, SMARCA4, SMARCE1, and ARID1A.
American journal of medical genetics. Part C, Seminars in medical genetics 2014 Sep 166C (3): 262-75. Kosho Tomoki, Okamoto Nobuhiko, |
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SMARCB1 mutations in schwannomatosis and genotype correlations with rhabdoid tumors.
Cancer genetics 2014 Sep 207 (9): 373-8. Smith Miriam J, Wallace Andrew J, Bowers Naomi L, Eaton Helen, Evans D Gareth |
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Multigene mutational profiling of cholangiocarcinomas identifies actionable molecular subgroups.
Oncotarget 2014 May 5 (9): 2839-52. Simbolo Michele, Fassan Matteo, Ruzzenente Andrea, Mafficini Andrea, Wood Laura D, Corbo Vincenzo, Melisi Davide, Malleo Giuseppe, Vicentini Caterina, Malpeli Giorgio, Antonello Davide, Sperandio Nicola, Capelli Paola, Tomezzoli Anna, Iacono Calogero, Lawlor Rita T, Bassi Claudio, Hruban Ralph H, Guglielmi Alfredo, Tortora Giampaolo, de Braud Filippo, Scarpa Al |
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Genotyping cancer-associated genes in chordoma identifies mutations in oncogenes and areas of chromosomal loss involving CDKN2A, PTEN, and SMARCB1.
PloS one 2014 9 (7): e101283. Choy Edwin, MacConaill Laura E, Cote Gregory M, Le Long P, Shen Jacson K, Nielsen Gunnlaugur P, Iafrate Anthony J, Garraway Levi A, Hornicek Francis J, Duan Zhenfe |
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Loss of
Neurology India 0 67 (6): 1492-1497. Malgulwar Prit B, Kakkar Aanchal, Sharma Mehar C, Ghosh Ranajoy, Pathak Pankaj, Sarkar Chitra, Suri Vaishali, Singh Manmohan, Kale Shashank S, Faruq Mohamm |
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- Page last updated:Jan 19, 2021
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